Monoazo and disazo triazine dyes



PatentedJulif i solubility in water and a 2-halogen-4-amino-l:3:5-triazine radical, which is bound in the 6-positionthrough an amino bridge, advantageously an amino bridge of the formula n-IHIn-l to the radical of a diazo-component, in which n represents a positive whole number and of which the amino group bound in the 4-position of the triazine nucleus is a free amino group or the radical of an amine which triazine yestufi with ammonia or with an amine contains at most twelve carbon atoms and, if ,it 0011; tains an aromatic nucleus, also contains a carboxylic acid or sulfonic acidgro'up. The dihalogen-triazine dye}: stufis to be used as starting materials can be made by" methods -in themselves known by reacting an azo-dye-f' stuff, which contains at least two strongly acid groups: imparting solubility in water and anacylatable I group in the radical of the di-azo componen'o'with cyanuric chloride (2:4:6-trichloro-1:3z5-triazine)" in 'at least equimolecular proportions, or those starting dye stuffs can be obtained from dyestutfflcomponents which contain the appropriate dichlorotriazine residue. 1

For preparing the azo-dyestufis used as starting matea, rials, which contain the acylatable amino groupi'n the diazo-component, there may be used, for example, dlflZQ-a components of monoacyl-derivatives of aromatic diamines,v for example, monoacyl-derivatives of- 4:4'-diamino.-di

0 phenyl-3-sulfonic acid, 4:4'-diaminostilbene-2:2'-disul=' tonic acid, 4-(4-aminobenzoylamino)-l-aminobenzene-2- sulfonic acid, 1:3- or 1:4-diaminobenzene, 1,:4-diaminobenzene-Z-carboxylic acid, 1:3-diaminobenzene-4-sulfonicj acid or 1-:4-diaminobenzene-3-sulfonic,acid, 2-methoxy-' 1:4-diaminobenzene 5-sulfonic acid, of which the acyl; radicals are hydrolyzed, after the coupling, to liberate the amino group.

contains at most 12 carbon atoms and, if it contains an aromatic ring, also contains an acid group imparting solubility in water, namely, a carboxylic acid and/or sulfonic acid group.

The invention provides more especially dyestufls which contain at least two sulfonic 'acid groups and correspond to the formula. i

in which X represents a 2-chloro-4-amino-1:3: 5 triazine radical, D represents the radical of a'diazo-component As coupling components for this purposethere may be used compounds capable of coupling, which are" free from acylatable amino groups, for example, B-keto-car-j boxylic acid esters or amides capable of'coupling in the; .a-position, for example, acetoacetic acid arylides, pyraz -f lones, especially 5-pyrazolones, capable of coupling in th 1 4-position, such ;as 3-methyl-5-pyrazolone, l-phenyl-fi-p methyl-j-pyrazolone, 1-phenyl-3-methyl-5-pyrazolone-2-, -3-,o'r' T4- sulfonic acid, l-phenyl-S-pyrazolone3-carbox ylic acid, 5-pyrazolone-3-carboxylic acid amide, barbituricf whichmaycontain an azo linkage, and A repre sents the I 40 radical of a coupling component, and in which the amino-- group'boun'd in-the 4-position of the triazine nucleus contains at most 12 carbon atoms and, if it contains an" aromatic ring, also containsa sulfonic acid and/or carboxyl'ic acid group. I

The characteristic triazine grouping is bound in the dyestufi' molecule to the radical of the 'diazocomponentr through an amino bridge which is bound directly or through a bridge member, for example, through an alkylene radical or an SO group, to the radical D of a dia'zo component. The radical D may be an unsubstituted phenylene radical or a methyl-, alkoxy-,'chloro- 'or nitro-T phenylene radical," or a larger radical, for 'example,"a naphthalene radical or a bicyclic rad'c'al 'which may" contain anazo linkage. I 1 I -f I, I

' In addition tothe above defined triazine grouping the dyestufis of this invention jc'ontain at'least two strongly acid groups imparting solubility in water, suchas car boxylic acid groups or above all sulfonic acid groups. Advantageously, the dy'estufis contain more than one such group per azo linkage, that is to say, at least two suchgroup's in a monoazo-dyestufi and atleast'three such groups in a disazo-dyestufi. These groups imparting solubility in water may be distributed in any manner in: the dyestutf molecule, but one such group must be present in the triazine radical, if the latter contains an aryl'amino group. i j a v The dyestuifs of this inventioncan be made by starting from an appropriate dyestufi, obtainable by methods in themselves known, which contains a dihalogem, andespecially a 2:4-dichloro-1:3:'5-triazine radical, and rea ting'one ofthe two chlorine atoms, in the dichloro-;

acids, hydroxyquinolines such as 8-hydroxyquinoline, 2: dihydroxyquinoline and phenols, such as para-cresol, 4-" acetylamino l-hydroxybenzene, 4 nlethyl-2-acetylamino-l hydroxybenzene, 2carboxy-l-hydroxybenzene, naphtholsj droxynaphthalene sulfonic acid amide, andabove alli amino and/or, hydroxynaphthalene sulfonic acids or theirj N-alkylor N-aryl-deriv'atives, such as 1-hydroxynaphtha- 5 lene-3-, -4-, -5- or -8-sulfonic acid, 2-hydroxynaphtha-j;

,naphthalene-3:6 disulfonic acid, Z-hydroxynaphthalenewor ethane sulfonyl, para-toluene sulfonyl or chlorobenzene sulfony-l group or a carbomethoxy or carbethoxy: group or an acyl radical derived from a cyanuric acid for example, a radical of the formula /N Ii in which both substituents Y represent halogen atoms or hydroxyl groups or amino groups, especially substituted amino groups. There may also be used as coupling components 5 5-dihydroxy-2 2-dinaphthyl-urea-7 :'7''disul 'l fonicacid or 5:5'-dihydroxy-2:2'-dinaphtliylamine 7;7

disulfonic acid, which coupling components, like I-amino- 8' hydroxynaphthalene-3 :6-disulfonic acid, may, if desired,

be coupled twice with the aforesaid diam-components,

and also compounds capable of coupling which contain an azo linkage, for example, monoazo-compounds obtainable, for example, by coupling'a simple diazo-compound o'f'the benzene or naphthalene series (for example, diazotized naphthylamine, anilines, such as chloroor nitroanilines, toluidines, aminobenzene sulfonic acids, chloroor nitro-aminobenzene' sulfonic acids, aminobenzoic acids,

nitro-amino-benzoic acids or nitroa'minophenols, etc.) in' an acid medium with 2-amino-5-hydroxynaphthalene-7- sulfonic acid, or 1-hydroxy-8-aminonaphthalene-3:6-disulfonic acid.

Inv this case also there are coupled together only such' starting materials as lead to the formation of amino-a20- dyestuffs containing at least two groups imparting solubility in water.

The condensation of the amino-azo-dyestufis obtained from these components and containing in the radical of the diazo-component anacylatable amino group with cyanuric chloride is carried out in such manner that two exchangeable halogen atoms remain in the condensation product obtained, and one of which halogen atoms is exchanged in the process of this invention for the radical ofanamino-compound of the kinddefined above. As such amino compounds there are used, apart from ammonia, amines such as methylamine, dimethylamine, ethylamine, diethylamine, isopropylamine, butylamine, hexylamine or cyclohexylamine, and also fl-chlorethyb amine, methoxyethylamine, 'y-methoxy-propylamine, eth-. ano'lamine, propanolamine and acylatable amines such. as acetamide, butyric acid amide, urea, thioureaand toluene, sulfonic acid amide, and also glycine, aminocarbonic' acid esters, such as the methyl or ethyl ester,'. aminoaceacid ethyl ester, amino-acetamide, hydrazine, phenylhydrazine sulfonic acids, th-iosemicarbazide, and l-amino benzene-2:5-disulfonic acid, 1-arninobenzene-2-, -3'- or"-4- sulfonic acid,aminonaphthalene monoor di-sulfonic acid, amino-diphenylsulfonic acids, B-aminoethane sulfonic acid and N-methyl-aminoethane sulfonic acid.

Thecondensation of these amino-compounds with die halogen-triazine dyestuffs is advantageously carried out with the use of an acid-binding agent such as sodium acetate, sodium carbonate or sodiumhydroxide and under conditions such that the vfinal product contains an exchangeable halogen atom, that is to say, for example, in an organic solvent or at a relatively low temperature in. i

an aqueous medium.

The-azo-dyestufifs of this invention canalso be made by amodification of the process described above. this. modification the azo-dyestuff used as startingmaterial for. preparing the dichloro-triazine dyestufi', and which contains at least two strongly acid group's imparting.

solubility and an acylatable amino group in the radical amino group in the radical of the'diazo component, or advantageously with the' diazo-components which are suitable for making the aforesaid dyestuifs and which contain an acylatable amino group in addition to the group capable of leading to dyestuif formation.

As examples of diam-components so obtainable, which contain a triazine. radical of the above kind, there may be mentioned'the secondary condensation products of one and SOaH

In making the dyfiistufis ofrthis invention by condensing one of the aforesaid amino-azo-dyestuffs with cyanurie.

chloride-and with a-simpler amino-compound of the kinddefined above; it is-generally' possible to carry out the.

steps" of the condensation'in either order of'succession, On'the-other hand, in making the dyestuffs bythe cou-\ pling procedure it is generally of advantage to "carry out r the condensations required for making the secondary condensation product tobe used as diazo-component by first forming the monoamino-dihalogen-triazine and subsequently condensing-it with the required diazo compoof. the diazo-component for example, an amino-azo dye-l stufiobtainable from the, components mentioned above,

is condensed with a 4:6-dihalogen-1:QES-triazine which contains in the 2-position a free amino group or the radical'of an amine containing at most 12 carbon atoms, and which, if it contains an aromatic ring, also contains an acid group imparting solubility in water, namely a carboxylic acid and/or sulfonic acid group.

The dihalogen-triazines of the aforesaid constitution can be prepared by methods in themselves known from cyanuric halides, such as cyanuric bromide or cyanuric chloride, by reacting, for example 1 molecular proportion of cyanuric chloride withll molecular proportion of ammonia or 1 molecular proportion of an amine of the kind. described above. In order to prepare the azo-dyestuffs of this invention the dihalogen-triazine compounds so, obtained are condensed with amino-azo-dyestuifs of the kind defined above, which contain two strongly acid Notwithstanding the presence of a labile halogen atom intthe' dyestufls' of .thisinvention they can be isolated and worked up into'useful dry dyestufi preparations, without losing their'valu'able properties. The dyestuffs are advantageously isolated at as low a temperature as possible.

by salting, out and filtration. The filtered dyestutfs may beudried, if desired, after the addition of an extender. The-dryin'gis preferably carried *outat not too high a temperature. and under reduced pressure. In certain cases dry preparations can be obtained directly by spray dryingthe entire mixture in which the dyestutf is prepared, that'is to say, without isolating the dyestufi.

The new dyestufls are suitable for dyeing or printing ai'veryvwidevariety ofmaterials, especially cellulosecontaining materials of fibrous structure, such as linen,

regenerated.cellulose'and above all'cotton. They are. especially well suited for dyeing by the'so-called pad' dyeing process, in whichth'e goods areimpregnatedwith an aqueousssolution ofthedyestuff, which may 1 also contain. a. salt, and the dyestufl is" fixed on the material with the. aid of heat, after treatment. with" any alkali or in the presenceipf an alkali... 'p oce -s drt i y ing.

5. method, which canbe used with many of the dyestufis of this invention, and also printing processes yield dyeings or prints which are generally distinguished by the purity of their tints, their good fastness to light and above all 6 The following examples part-s and percentages being by weight:

Example 1 their excellent fastness to washing. 5 31.65 parts of the secondary condensation product from When the dyestuffs contain groups capable of forming 1 mol of cyanuric chloride, 1 mol of 1:3-diaminobenzene-1 metal complexes, for example, ortho:ortho'-dihydroxy 4-sulfonic acid and 1 mol of ammonia are stirred in 300 azo-groupings or ortho:ortho'-hydroXy-carboxy-groupings parts of water, 300 parts of ice and 20 parts of hydrosuch as are present, for example, in salicylic acid radicals, chloric acid of 30% strength, and diazotized at 02 C. the dyeings obtained with these dyestuffs may be treated with 25 molar parts of a 4N-solution of sodium nitrite. with an agent yielding metal, for example, an agent To the diazo-suspension so obtained, which is acid to yielding chromium, or advantageously an agent yielding Congo, there are added 30 parts of sodium acetate nickel or copper. The treatment with the agent yielding (cHscozNa'sHzo) metal maybe carried out by methods in themselves .e 1' .known. If desired, very valuable dyeings can be obtained andothen the mlxture 15 added to a ,solutlon cooled m by the process in which a dyeing produced with the metali palzts of l'benzoylamlno's'hydrmfynaph' free dyestufi is after-treated with an aqueous solution thalenif'iifidlsulfmw and (Present as the alkah f which contains a water-soluble copper compound, espem 400 Parts of Water and P2915 of calcmed cially a water-soluble complex copper compound, and a sodlum i f When the q p 1s the basic formaldehyde condensation product of a compound dyestufl 1S preclpltated by F addmim of potgssmm containing at least once tha atomic grouping ride, filtered off, washed with potass um chloride solution, 5 1 i and dried at 70 C. in vacuo. It dissolves in: cold water; with a bluish red coloration and dyes cellulose fibers by the so-called pad dyeing process fast bluish red tints. 5 By the same method similar dyestuffs are obtained by N coupling the secondary condensation products mentioned in column I of the following table .with the couplingor of a compound, such as cyanamide, which is easily components given in column II, and which dyestuffs dye convertible into a compound containing such an atomic cotton by the so-called pad dyeing process the tints given grouping. in column III, which have good properties of wet fasmess;

I II III H0 NH-COCH: red. C N\ 1 mN-c (|fNH soaH \C/ NH: H038 $0315 H0 0-0211 no; N\ 2 HzN-(lJ (|'|J-NHQSO@H NH: H0; sonar 01 N\ H(|) 3 HmsONH-O C-NHGSO H CN scan yellow:

I ll N\ /N 111E HC\ 31 o o= ll 33H:

HO 50311 N\ l r 4 HaN O (i NH 803E bluish red:

N NH 7 J1 NH-COCH:

5 HzN-O CNH scan C-NO-SOaH yellow:

I ll N NH. H0 v a v C=N All H:

N a HNO CNH 50311 no m \C/ NHQ NH-COCH;

illustrate the invention, the- 19 Example 2 8.76 parts of the dyestuif of the formula "SOaH are dissolved inthe form of the sodium salt in 300 parts of water, and 3.18 parts of sodium carbonate are added. The solution is cooled to 05 C. and there'is added a solution of 3.7 parts of cyanuric chloride in 50 parts of acetone. The w o e is stirred for 2-3 hours at -5. C4! then 50 parts of an aqueous solution containing 0.8 part of ammonia are added, and the whole is stirred for a further 2 hours at 40-45 C. The dyestutf is then salted out with 100 parts of sodium chloride.

The product is filtered off at room temperature, washed with saturated sodium chloride solution, and dried at 45 C. in vacuo. There are obtained 1-9.9 parts of a red powder which dyes cotton from an alkaline bath-having a high'concentration of a salt bluish red tints.

A dyestuif which dissolves well in water and dyes cotton bluish red tints is obtained by condensing the aminoazo dyestufi of the above formula with the primary condensation product of Z-aminobenzene-l-sulfonic acid and cyanuric chloride. This dyestuif can also be prepared by coupling 2-amino-8-hydroxynaphtha1e116-6-sulfonic acid in an acid medium with the diazo-compound of the secondary condensation product obtained from 2-aminoben-. zene-l-sulfonic acid, cyanuric chloride and 1:4-diaminobenzene-3-sulfonic acid. a

Example 3 47.25 parts of the secondary condensation product ob-. tained from 1 mol of cyanuric chloride and 1 mol of 1-. aminobenzene-Z-sulfonic acid and rmol of 1:3-diaminobenzene-4-sulfonic acid are stirred in 300 parts of water, 300 parts of ice and 20 parts of hydrochloric-acid of 30% strength, and diazotized at 8-l0 C. with 5 Parts by volume of a 4 N-solution of sodium nitrite.

The diazo-suspension so obtained, which is acid to Congo is then added to a solution of 23.9 parts of 2-. amino-8-naphthol-6-sulfonic acid in 1200 parts of water and 60 parts of sodium acetate (CH CO Na3H 0). The whole is then stirred at 25-30 C. until the coupling is complete, and the dyestuif is precipitated by the addition of sodium chloride, filtered OE, and dried in vacuo at 70-80 C. The dyestufl? dissolves in water with a red coloration and dyes cellulose fibers from an alkaline bath containing a salt red tints which are fast to light and washing.

Dyestuifs having similar properties are obtained by condensing cyanuric chloride with 1:3- or 1:4-aminoben-. zene sulfonic acid or 1:2-, 1:3- or lz laminob'enzene carboxylic acid or ammonia, instead of-l-aminobenzene-L sulfonic 'acid. Y

Example 4 31.6 parts of the triazine of the formula (I?! C i n I V HN- I are suspended in 500 parts of water, the pH value of the suspension isadjusted to 8.5. with sodium hydroxide solu- 20 tion, 6.9 parts of sodium nitrite in the form of an'aqueous solution are added, and the whole is poured into 50 parts of ice and parts of hydrochloric acid of strength. When the diazotization has ceased, coupling is carried out with 22.3 parts of l-aminonaphthalene-7-sulfonic acid dissolved in the form of the neutral sodium salt in water. The solution is neutralized to a pH value of 4.0 with sodium acetate. When the coupling is finished, the pH value of the mixture is adjusted to 8.5 with sodium hydroxide solution, 6.9 parts of sodium nitrite are added in the form of an aqueous solution, and the whole is poured into parts of hydrochloric acid of 30% strength at a temperature of 0 C. The color of the diazo-compound is orange-brown. Coupling is carried 'out with a solution of 28.1 parts of -2,-acetylarnino S-hydroxynaphthalene-6-sulfonic acid in 200 parts of water and parts of sodium carbonate. After 24 hours the dyestulf is separated and dried. It dyes cottom from a salt-containing alkaline bath weal; reddish blue tints.

Instead of Z-acetylamino-8-hydroxynaphthalene-6-sulfonic acid other azo-components may be used, for example, the following:

(a) l-acetylarnino-8-hydroXynaphthalene-3 :6-disulfonic acid, which yields a pure neutral blue dyestuif,

(b) The triazine obtained by condensing 1 mol of cyanuric chloride with 1 molof 'l-arnino-8-hydroxynaphthalene-3z6-disulfonic acid, and 1 mol of ammonia, which has the formula and yields a pure neutral blue dyestulf.

(c) 2 acetylamino 5 hydroxynaphthalene 7 sulfonic acid, which yields a reddish blue dyeing dyestufl.

(d) 1-hydroxynaphthalene-4-sulfonic acid, which yields a dyestuff producing reddish navy blue tints.

(e) The pyrazolone of the formula IOaH H Example 5 31.6 parts of the triazine of the formula are diazotized in the manner described in Example 4.

As the. coupling component there is used the monoazo- 54"-8;-pa rts of.this,fmonoazo-dyestuffv are 'dissolvedin 200;

partsof water; 25;.parts'of sodium bicarbonate .arel added, the;;whleis cooled .WlthjiCeTIO' 0 C.. and. the diaz a suspension of the aforesaid triazine is: run in:.while stirring? vig'Qrously..:;1 Aft'erstirringthezmixture for several hours,

theidiSaZQ-edyestufif formed is.- precipitated by the addition ofsodium; chloride,xfiltered 201i and'dried- Thewresultingdyestuff dyes-cellulose fibers from strong saltecontainingzalkalines baths, slightly greenish blue tints whichrarezfastto washings 1 A; simiiandyestuif is obtainedzbyusing a triazineof' '22 out with'2213 parts 'of'1-arninonaphthalene 7=sulfonic acid dissolved in water in the form" of itsneut'ral' sodiunr saltfi The mixture is neutralized to a pH-Valiie of 4L0 with sodium. acetate. i When the couplingfis" finished; the pH- value of the mixture is adjustedito 8.5ijwith"caustic 'soda solution, 6.9 parts of sodium nitrite are iadd'edin the formof an aqueous. solution, and 'thewholeis'poured' into:

parts of hydrochloric acid of. 30%: strength-at 0 C;

The color of the diam-compound is orange-brown;

Coupling is carried out with a'solut'ion'. of 22.3 parts er 1-aminonaphthalene-7-sulfonic' acid'in thez'form' ofgits neutral sodium salt dissolved in 300 parts. of water After 24 hours, the dyestufl is separated and dried. The dyestuif dyes cotton from salt-containing alkaline baths the,..abovegformula in Whicl'rthe.'NH group: condensed 5 blue-violet tints which are fast to washing.

tothertriazine ring; is replaced by-the residue of l-aminobenzeneA-sulfonic acid onthe' residue of Z-aminonaphthalene-4z8-disulfonic'acid.

fi n 33.6 partsofi' the triazine of the formula 21 are diazotized in the manner described in Example 4, and coupled with an aqueous solution of 23.9 parts of. 2-

amino-S-hydroxynaphthalene-7-sulfonic acid in 500 parts of water and 30 parts of sodium carbonate. when the coupling is finished 6.9; parts of sodium nitrite are added the whole is; poured into a quantity of ice and parts of hydrochloric acid of.30.% strength. {I'hediazotizatiomofitheamino-azo-dyestufif is completeafter stirring the mixture for several hours. The dia zo-cornpound Example 7 31.6 parts of the triazine of the formula We. anagram.

are suspended in 500 parts of water, the pH value of the mixture is adjusted to 8.5 with caustic soda solution, 6.9 parts of sodium nitrite are added in the form of an aqueous solution, and the Whole is pouredinto 50 parts of ice and 25 parts of hydrochloric acid of 30% strength. As soon as the diazotization is finished, coupling is carried Example '8 785 parts of the dis'azo dyestuif'of the formula" soin aqueous'solution of'25 parts of l-naphthol-4 s'ulfonicacid;

which contains an excessof sodium carbonate. Atterl24 hours. the. trisazo-dyestuff ,Iformed. is] precipitatedfbyl "the addition of 'sodiuni chloride, filtered. ofi'jandl dried; It dyes f cotton from salt-containing, alkaline baths dark. blue.

tints which are very fast-to Washing.

Ema. '9 33.6 parts of the triazine of the formula 0H: Qatar -G sele sodium nitrite' 'are added, and 25"partsof hydrochlo acid of 30% Strength are introduced. As soon as"the' diazotization is finished, coupling is carried out with 46.7 parts of the condensation product from 1 mol of cyanuric chloride with lmol of l-amino-8-hydroxynapthalene-3:6-

disulfonic acid" of the formula in .4Q6 parts ofzwaterl and 25 parts ofisodium carbonate; As soon asthe coupling'is finished, 40 parts of an aqueous solution of ammonia of 172% .strengthgare. added, the

stirred for. several. hours. atYOP; Cl, Ihe {diaz'ocoiii pohnd so obtained isadde'd; for the, purpose of coiuplmg. to. an,

aresuspended in 400 parts oiwater and ice, 6.9, parts of.

' yields a fast orange-red 7 whole is-heated for '2 hours at 40-45 C., and the prod-v uct is separated and dried. .The dyestutf so obtained dyes cellulose fibersfrom alkaline baths having a high concentration of a salt'very pure red tints of excellent fastnessto washing and light.

- .Thefsame'dyestuif can be obtained by using as cliazo component a Itriazine of the first formula given above, but in which one. of the twola-bile chlorine atoms has been exchanged for an -NH group.

1 Instead; of the. diazo-compound of the formula first given above there maybe used the secondary condensation Y product of the formula V (.61

N/ UN I 2 nmsQ-avu-b I ii-NH-Q-sOm A similar dyestufi is obtained 'by using, instead of the above diazo-compound, the triazine of the formula nos 1 NH,

yields a pure 'fast' orange tint, and the dyestufi of the.

sm e I Example 62.9 parts of the dyestufi of the formula.

Y e no a prepared in known mannerby-coupling diaz otized 4- nitro-4'-aminostilbene-2:2'-disulfonic acid with phenol, esterifying the resulting para-hydroxy-azo-dyestutf with para-toluene sulfo-chloride and reducing the nitro-azodyestuif to the amino-azo-dyestuif by means of an aqueous solution of sodium hydrosulfidc, are dissolved in the form of the neutral sodium salt in 400parts of water. The resulting solution is added, while stirring vigorously, at 0 C. to a reprecipitated fine suspension of 18.5 parts of cyanuric chloride in water. By simultaneously introducing dropwise a 1 N-solution of sodium hydroxide the pH value of the reaction mixture-is maintained constant between 5.0 and 6.0 After about one hour the condensation is finished, and the-primary condensation product is in solution. There is then added an aqueous solution which contains 4 parts of ammonia. The reaction mixture-is heated to 40 C. and stirred for 2 hours at that temperature. By the addition of sodium chloride the secondary condensation product is precipitated at a pH value of 7.5, filtered 01f and dried at C. The dyestufl is a yellow powder which dyes cellulose fibers from alkaline baths having a high salt concentration full yellow tints which are fast to washing.

A similar yellow dyestufi is obtained by using as starting material an amino-monoazo-dyestufiof the formula HaN-QCHAJHQ 03 7 Boss or l NHQGmoH-Q SOaH SOaH N=N O CHI- and otherwise proceeding in the manner described in this example.

and reacting it at about 40 C. with the amino-a20- dyestufi.

f! v i. our no. V a J J "a "2s Example 11 2 parts of the dyestuif of the formula are dissolved in '100 parts water by the addition of 1 part of sodium hydroxide. A cotton fabric is impregnated with the solution at room temperature, then squeezed to a Weight increase of 70% and dried. The fishermen steamed for 60 seconds; rinsedsoapedfor 15 minutes in a boiling solutionof about 0.3% strength of a non-ionic detergent, rinsed anddried. There is obtained a blue-red dyeing which is fast to washing and light.

V Examplei12 2 parts of the dyestulf of the formulaare dissolved in 100 parts oi wateh zA ljabric of staple fibers of regenerated cellulose impregnated with the resulting solution so that its weight increase amounts to 75%, and is then dried.

The fabric "'is subsequently imprfgnated with a solution having a temperature of 20 C; which contains, per liter, 10 grams of sodium hydroxide and 300 grams of sodium chloride, the fabric is squeezed to a weight increase of75% and the dyeing is steamed for 60 seconds at 100-101 C., rinsed, soaped for a 4 hour in a boiling solution of 0.3% strength of a non-ionic detergent, rinsed and dried. There is obtained a yellow dyeing which is fast to light and washing.

By using, instead of a fabric of staple fibers of regenerated cellulose, a cotton fabric, a similar good result is obtained.

What is claimed is:

1. A water-soluble azo dyestufi of the formula V wherein A represents the radicalof a coupling component containing a water-solubilizinggroup and also a member selct'edfrom the group consisting of the hydroxyl and amino groups, said radical being bound to the adjacent azo linkage in a position vicinal to said member and being selected from the group consisting of pyrazolone, quinoline, benzene and naphthalene radicals, n represents a whole positive number up to 2, R represents a member selected from the group consisting of a benzene and a naphthalene radical, R represents a benzene radical, and Y represents a member selected from the group consisting wherein A represents the radical of a coupling-component 26 an :aromatic at most bicyclictaminia sulfonic; acid bound to the triazine nucleus by its amino -group,-anditherradical of an aminobenzene-carboxylic acid bound to the triazine nucleus by its amino group.

2. An azo dyestuif according to claim 1, wherein n is 1.

:35 Awater soluble monoazo dye's'tufl" which in its free acid state corresponds'to the formula wherein A represents the radical of a coupling component containing an hydroxyl group and at least one member selected from the group consisting of a sulfonic and a carboxylic acid group, saida radicalcbeing' bound? torthefiazb linkage in:- vicinalspositidnitoe-saidmhydroxy group and being selectedsfrom therkgroupaconsisting g bfr pyrazolone, quinoline, benzene and naphthalene radicals.

4. A water-soluble monoazo dyesfufi which in its free acid state corresponds tqthe-formulacdntainin'g an 'hydroxyl grou'p andat least one member selected from the group' consisting o a sulfoni'c and a carboxylic acid group, said radical being bound to the azo linkage in vicinal positions to said hydroxy group and being selected from the group consisting of pyrazolone, quinblineibenzene and naphthalene radicalsgandy represents-theradicalmf-anaminobenzene sulfonic acid.

"5: A water-soluble monoazo dyest-utf which in itstree acid state corresponds. to the formula 6. A water-soluble monoazo dyestulf which in it s free acid state corresponds to the formula of the NH group, the radical of a primary aliphatic 2,945,021 27 o a 7 28 wherein A represents theradical of a hydroxynap'hthalene wherein R represents a benzene radical, one of the Xs a sulfonic acid bound to the azo linkage in vicinal position hydrogen atom and the other X a sulfonic acid group.

' 10. The monoazo dyestutf which in its free acid state corresponds to the formula H NBC--00 N-C 04m -N N- 50311 HOsB- scan 03H a A $1:

of the hydroxyl group and Y represents the radical of 11. The lnonoazoidyestutf which in its free acid state an aminobenzene sulfonic acid bound byits amino group corresponds to the. formula 7 o1 p v C-N BIN-#0 C--NH N=N-O 4083 no s -so n to the triazine nucleus. 3 i v 12. The monoazo dyestufi which in its free acid state 7. A water-soluble monoazo dyestuif which in its free corresponds to the formula acid state corresponds to the formula a I Y v v v 7 NH,

35 p t NH-o (J-NH: N=N a a N it o H0 40 03H in wherein A represents the radical of an acylamino hyi droxynaphthalene disulfonic acid bound to the azo Iink- H 7 age in a position vicinal to the hydroxy group and Y the gmup' r 8. A water-soluble monoazo dyestufl which 111 its free acid state corresponds to the formula N H V H0 H v a N y N N' \O/ H NH-Aoyl A som s .H 1

wherein Acyl represents the radical of a lower carboxylic 13. The monoazo dyestuff which in its free acid state acid bound by its --CO group to the -'-NH-- group. corresponds to the formula 9 A water-soluble monoazo dyestuff which in its free acid state corresponds to the formula no HN-OO-R 14. The monoazo dyestutf which in its free acid state corresponds to the formula References Cited in the file of this patent UNITED STATES PATENTS TED STATES ATENT FFICE ETIHCATE 5 QTN I Patent NOQ 2,945,021 July 12, 1960 Alfred Fasciati et al.

It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read. as corrected below Column 28 lines 34 to 441, the formula should appear as shown below instead of as in the patent:

N NHZ -NH-c \CNH N N N 50 1-1 SOSH \C SO3H SEA L) Attest:

ERNEST W. SDER Attesting Uffieer DAVID L. LADD Cossioner of Patents UNITED STATES PATENT OFFICE Certificate of Correction Patent No. 2,945,021 July 12, 1960 Alfred Fasciati et a1.

It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.

Columns 9 and 10, opposite 18, under the column headed II, the third formula should appear as shown below instead of as in the patent:

column 23, lines 47 to 52, the left-hand portion of the formula should appear as shown below instead of as m the patent:

same column 23, lines 57 to 63, the right-hand middle portion of the formula should appear as shown below instead of as in the patent:

HOIS

column 25, lines 24 to 32, Example 12, the left-hand portion of the formula should appear as shown below instead of as in the patent:

N N'Hg-C C- r e 9 In column 27, lines 4A and 45, strike out and Y the NH group.

Signed and sealed this 30th day of May 1961.

Attest: ERNEST W. SWIDER, DAVID L. LADD, Attestz'ng Oficer. dam/mission of Patents. 

1. A WATER-SOLUBLE AZO DYESTUFF OF THE FORMULA 